Bis(pyridine‐2,6‐dimethanol‐N,O,O′)cobalt(II) and ‐copper(II) disacchar­inate dihydrate: three‐dimensional structures with extensive hydrogen bonds and aromatic π–π‐stacking interactions

Bis­(pyridine‐2,6‐di­methanol‐N,O,O′)­cobalt(II) disaccharinate dihydrate, [Co(C₇H₉NO₂)₂](C₇H₄NO₃S)₂·2H₂O, (I), and bis­(pyridine‐2,6‐di­methanol‐N,O,O′)copper(II) disaccharinate dihydrate, [Cu(C₇H₉NO₂)₂](C₇H₄NO₃S)₂·2H₂O, (II), collectively [M(dmpy)₂](sac)₂·2H₂O (where M is Co^II or Cu^II, sac is the saccharinate anion and dmpy is pyridine‐2,6‐di­methanol), are isostructural. The [M(dmpy)₂]²⁺ cations exhibit distorted octahedral geometry in which the two neutral dmpy species act as tripodal N,O,O′‐tridentate ligands. The crystal packing is determined by hydrogen bonding, as well as by weak pyridine–saccharinate π–π‐stacking interactions.     

Theoretical demonstration of the hybrid focusing points of sonic crystal flat lenses and possible applications

We demonstrate the hybrid focusing points of sonic crystals for a multi-source array applied to flat sonic crystal lenses. The contributions of different point source couples form hybrid focusing points. Ray-trace analyses are conducted for acoustic flat lenses with multi-source configurations. The finite-difference time-domain (FDTD) simulation of flat lenses with multi-source configurations demonstrates the establishment of pure and hybrid focusing points in a pyramidal constellation. The number of focusing points in the pyramidal constellation depends on the number of point sources. We propose an acoustic device for fine-tuning the location of a far-field hybrid focusing point and discuss its benefits for acoustic energy focusing application.     

Utilization of smart hydrogel-metal composites as catalysis media

Various metal nanoparticles such as, Cu, Co, Ni, and Fe were prepared inside poly(1-vinyl imidazole) p(VI) hydrogel by the absorption of the corresponding metal ions from aqueous solutions and the reduction with suitable reducing agents such as NaBH(4) and/or NaOH. TGA and ICP-AES were used to determine the metal particle content of p(VI)-M (M: Cu, Co, and Ni) composites. The prepared hydrogel-metal nanoparticle composites were proven to be resourceful as reaction container for the catalysis of various organic reactions. It was illustrated that p(VI)-M hydrogel-metal composites can be successfully used in the hydrolysis of NaBH(4) for the generation hydrogen form NaBH(4) and NH(3)BH(3). Additionally, p(VI)-M composites were also illustrated in the catalysis of different organic reactions; e.g., these hydrogel-M are very effective in the reduction nitro aromatic compounds such 2-nitrophenol (2-NP) and 4-nitrophenol (4-NP) to their corresponding amine forms in the presence of aqueous NaBH(4). Various parameters in the catalysis of hydrogen production and 4-NP reduction were determined.     

Light sources generating far fields with tunable flat profiles

Planar, scalar, optical Schell-model, and quasi-homogeneous sources with correlations that are Fourier transforms of multi-Gaussian functions are introduced. It is demonstrated that far fields produced by these families of sources carry interesting characteristics, being flatlike with adjustable steepness of the edge. Beam conditions for such sources are also derived.     

On the mean and extreme distances between failures in Markovian binary sequences

This paper is concerned with the mean, minimum and maximum distances between two successive failures in a binary sequence consisting of Markov dependent elements. These random variables are potentially useful for the analysis of the frequency of critical events occurring in certain stochastic processes. Exact distributions of these random variables are derived via combinatorial techniques and illustrative numerical results are presented.     

Synthesis and Characterization of New 7‐Substituted 6,14‐Ethenomorphinane Derivatives: N‐{5‐[(5α,7α)‐4,5‐Epoxy‐3,6‐dimethoxy‐17‐methyl‐6,14‐ethenomorphinan‐7‐yl]‐1,3,4‐oxadiazol‐2‐yl}arenamines

In this study, (5α,7α)‐4,5‐epoxy‐3,6‐dimethoxy‐17‐methyl‐6,14‐ethenomorphinan‐7‐carboxylic acid hydrazide ( 5 ) was synthesized by the condensation of methyl (5α,7α)‐4,5‐epoxy‐3,6‐dimethoxy‐17‐methyl‐6,14‐ethenomorphinan‐7‐carboxylate ( 4 ) with NH₂NH₂⋅H₂O. The (5α,7α)‐4,5‐epoxy‐3,6‐dimethoxy‐17‐methyl‐6,14‐ethenomorphinan‐7‐carboxylic acid 2‐[(arylamino)carbonyl]hydrazides 6a – 6q were prepared by the reaction of 5 with corresponding substituted aryl isocyanates, and the N‐{5‐[(5α,7α)‐4,5‐epoxy‐3,6‐dimethoxy‐17‐methyl‐6,14‐ethenomorphinan‐7‐yl]‐1,3,4‐oxadiazol‐2‐yl}arenamines 7a – 7q were obtained via the cyclization reaction of 6a – 6q in the presence of POCl₃. The synthesized compounds have a rigid morphine structure, including the 6,14‐endo‐etheno bridge and the 5‐(arylamino)‐1,3,4‐oxadiazol‐2‐yl residue at C(7) adopting the (S)‐configuration (7α). The structures of the compounds were confirmed by high‐resolution mass spectrometry (HR‐MS) and various spectroscopic methods such as FT‐IR, ¹H‐NMR, ¹³C‐NMR, APT, and 2D‐NMR (HETCOR, COSY, INADEQUATE).     

A novel dual channel responsive zinc(II) probe

A novel compound, 1, which is based on a 1,10-phenanthroline scaffold with cofacial BODIPY units, is synthesized via a three-step reaction sequence. It is noteworthy that 1 can be utilized for both visual and turn-off fluorometric detection of Zn²⁺ ions in aqueous acetonitrile solution. The fluorescence response is based on cation-mediated oxidative photoinduced electron transfer (PET). The digital action of a two-input NOR logic gate is also demonstrated.     

Removal of Chromium Anions with Nanofiltration-Complexation by Using p-Sulfonated Calix[4]arene

This article describes the removal of chromium anions from aqueous solutions by using nanofiltration-complexation consisting of pilot-scale nanofiltration equipment (Osmonics Sepa CF Membrane Cell) and water-soluble p-sulfonated calix[4]arene ligand. For the determination of optimum removal conditions of the chromium anions, the effect of pH, ligand cavity size, and foreign anions on the retention of the chromium anions in nanofiltration-complexation system was also evaluated. The results showed that water-soluble p-sulfonated calix[4]arene was an effective and selective ligand for the chromium anions over Cl^? , SO₄ ^2 ?  and NO₃ ^?  anions in nanofiltration-complexation system at pH 9.4.     

Effective catalytic oxidation of alcohols and alkenes with monomeric versus dimeric manganese(II) catalysts and t‐BuOOH

Two new Mn(II) complexes, [Mn(C₆H₅COO)(H₂O)(phen)₂](ClO₄)(CH₃OH) ( 1 ) and [Mn₂(μ‐C₆H₅COO)₂(bipy)₄]?2(ClO₄) ( 2 ) (phen = 1,10‐phenanthroline; bipy = 2,2′‐bipyridine), were synthesized and characterized using UV–visible and infrared spectroscopies and single‐crystal X‐ray diffraction analyses. Complexes 1 and 2 have six‐coordinate octahedral geometry around the Mn(II) centre. Complex 1 is a monomer and consists of a deprotonated monodentate benzoate ligand together with two neutral bidentate amine ligands (phen) and a water molecule. Complex 2 has a dinuclear structure in which two Mn(II) ions share two carboxylate groups, adopting a two‐atom bridging mode, and two chelated bipy ligands. Both complexes catalyse the oxidation of alcohols and alkenes in a homogeneous catalytic system consisting of the Mn(II) complex and tert‐butyl hydroperoxide (TBHP) in acetonitrile. The system yields good to quantitative conversions of various alkenes and alcohols, such as styrene, ethylbenzene and cyclohexene to their corresponding ketones, and primary alcohols and 1‐octanol, 1‐heptanol, cyclohexanol, benzyl alcohols and cinnamyl alcohol to their corresponding aldehydes and carboxylic acids. Complexes 1 and 2 exhibit very high activity in the oxidation of cyclohexene to cyclohexanone (ca 80% selectivity) as the main product (ca 94% conversion in 1 h) and of cinnamyl alcohol to cinnamaldehyde (ca 64% selectivity) as the main product (ca 100% conversion in 0.5 h) with TBHP at 70°C in acetonitrile. In addition, optimum reaction conditions were also determined for benzyl alcohol with complexes 1 and 2 and TBHP. Copyright © 2016 John Wiley & Sons, Ltd.